Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.
Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.
The electronic medicines compendium (emc) no longer publishes a Summary of Product Characteristics for this product, which usually means it is no longer marketed in the UK. The patient leaflet below is kept for reference, but the product may not be available.
If you were prescribed this medicine, other products containing Metronidazole may still be available. Do not stop your treatment — ask your pharmacist or GP what to use instead.
for Your doctor has prescribed this gel for your skin condition, rosacea. helps to treat the pimples, pustules (spots) and redness found with this condition. Rozex contains the active substance metronidazole. Metronidazole belongs to a group of medicines called antiprotozoal and antibacterial agents and has been shown to help to control infection and inflammation in certain skin problems, such as rosacea.
e Rozex Do not use Rozex you are allergic to metronidazole or any of the other ingredients of this medicine (see section 6 for other ingredients). An allergic reaction may include a rash or itching. If you are affected by Cockayne syndrome. Cases of severe liver toxicity/acute liver failure, including cases with a fatal outcome, in patients with have been reported with products containing metronidazole. Cockayne syndrome nave Warnings and precautions Talk to your doctor or pharmacist before using Rozex.
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Rozex Always use this medicine exactly as your doctor had told you. Check with your doctor or pharmacist if you are not sure. Adults and the elderly First wash and dry the affected areas of your skin. Apply a thin layer of the gel to all the affected areas be careful also not to get it in your eyes. Rub the gel in well. Always replace the cap and wash your hands after use. Your gel should be used in this way twice a day, (morning and evening), or as advised by your doctor. Your doctor will decide how long you need to use Rozex to keep your rosacea under control. –
SGK
P Code: P202261-1 Description: ROZEX NF GEL 50 Market: GBR Article: Leaflet Designation: TBC Plan No: MT.09.DRA.0352.R03.2
Dimensions: Cutter Ref: Printer: Print Process: Print Spec:
180X315 N/A N/A
N/A
Pharma code: 2969
Service Order: 404324868 Version No: V1 Date: 17-10-2025 Operator: AD Barcode: N/A Mag: N/A BWR: N/A
Colours and Varnishes: PANTONE 432 U
EST.1981
Version No:
ARTWORK
NOTICE VERSO 180×315 PLAN n°
If you use more Rozex than you should or accidentally swallow the gel This product is for use on the skin only. Do not swallow it. If you accidentally do so, seek medical advice. If you forget to use Rozex worry if you forget to use your gel at the right time. Although this gel works best if you use it regularly as directed, When you do remember, start using it again in the same way as before. If you stop taking Rozex Rosacea may respond slowly to antibiotics. It is important that you continue using Rozex until your doctor tells you to stop. If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them. Common: may affect up to 1 in 10 people dry skin redness of the skin (erythema) itching of the skin (pruritus) skin discomfort (burning, pain of skin / stinging) skin irritation worsening of rosacea Uncommon: may affect up to 1 in 100 people numbness (hypothesia) and tingling (paraesthesia) in the fingers or toes metallic taste (dysgeusia) feeling sick (nausea) Not known: frequency cannot be estimated from the available data contact dermatitis swelling of the face peeling skin (exfoliation) If skin irritation should occur either use the gel a little less often or even stop using it until the irritation settles down. Seek medical advice from your doctor or pharmacist if necessary. Reporting of side effects you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at https://yellowcard.mhra.gov.uk or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects you can help provide more information on the safety of this medicine. –
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to store Rozex 5. How ta Keep this medicine out of the sight and reach of children. Do not use this medicine after the expiry date which is stated on the tube and carton. The expiry date refers to the last day of that month. Do not store above 25°C. Do not freeze. Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.
Rozex 6. Contents of the pack and other information –
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What Rozex contains The active substance is metronidazole. Each gram of Rozex contains 7.5mg of metronidazole. The other ingredients are carbomer 940, disodium edetate, methyl parahydroxybenzoate (E218), propyl parahydroxybenzoate (E216), propylene glycol (E1520), sodium hydroxide (for pH adjustment) and purified water. What Rozex looks like and contents of the pack Rozex is a clear to pale yellow gel which may turn to slightly brown colour over time. 40 g or 50 g tube, only on prescription from your doctor. Not all pack sizes may be marketed. It is available in g, Marketing Authorisation Holder and Manufacturer Limited, Evergreen House North, Grafton Place, London, England, NW1 Galderma Montdésir, Manufacturer: Laboratoires Galderma, Alby-sur-Chéran, 74540 France. This leaflet was last revised in October 2025.
GALDERMA SGK
P Code: P202261-1 Description: ROZEX NF GEL 50 Market: GBR Article: Leaflet Designation: TBC Plan No:
Colours and Varnishes: PANTONE 432 U
Dimensions: Cutter Ref: Printer: Print Process: Print Spec:
180X315 N/A N/A
N/A
Pharma code: 2969
Service Order: 404324868 Version No: V1 Date: 17-10-2025 Operator: AD Barcode: N/A Mag: N/A BWR: N/A
GALDERMA EST.1981
Version No:
ARTWORK
Rozex 0.75% w/w Gel comes as gel. Always follow the dose your doctor or pharmacist has given you, and read the leaflet that comes with the medicine.
The active substance in Rozex 0.75% w/w Gel is metronidazole.
Medicines with the same active substance, strength and form include: Acea 0.75% w/w Gel, Metrogel 0.75% w/w Gel. They are interchangeable only if your prescriber or pharmacist says so.
This leaflet reproduces the patient information leaflet approved for Rozex 0.75% w/w Gel, as published on the electronic medicines compendium (emc). The version printed inside your medicine’s packaging is the one that applies to you.
Whether a medicine is available over the counter or on prescription only depends on its licence. Check the leaflet, or ask your pharmacist — they can tell you straight away.
The text above reproduces the patient information leaflet approved for this medicine, restructured for easier reading.
Rozex Gel is indicated in the treatment of inflammatory papules, pustules and erythema of rosacea
Posology
For topical administration only.
The average period of treatment is three to four months. The recommended duration of treatment should not be exceeded. However, if a clear benefit has been demonstrated, continued therapy for a further three to four months period may be considered by the prescribing physician depending on the severity of the condition. In clinical studies, topical metronidazole therapy for rosacea has been continued for up to 2 years. In the absence of a clear clinical improvement, therapy should be stopped.
Older people: The dosage recommended in the elderly is the same as that recommended in adults.
Paediatric population: Not recommended. Safety and efficacy have not been established.
Method of administration
Rozex Gel should be applied in a thin layer to the affected areas of the skin twice daily, morning and evening. Areas to be treated should be washed with a mild cleanser before application. Patients may use non-comedogenic and non-astringent cosmetics after application of Rozex Gel.
Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
Metronidazole must not be used in patients with Cockayne syndrome. Cases of severe hepatotoxicity/acute hepatic failure, including cases with a fatal outcome with very rapid onset after treatment initiation in patients with Cockayne syndrome have been reported with products containing metronidazole for systemic use.
Contact with mucous membranes should be avoided.
Rozex Gel has been reported to cause lacrimation of the eyes, therefore, contact with the eyes should be avoided. If a reaction suggesting local irritation occurs patients should be directed to use the medication less frequently or discontinue use temporarily and to seek medical advice if necessary. Metronidazole is a nitroimidazole and should be used with care in patients with evidence of, or history of, blood dyscrasia. Exposure of treated sites to ultraviolet (e.g. solarium, sun-lamp) or strong sunlight (including sun-bathing) should be avoided during use of metronidazole. Metronidazole transforms into inactive metabolite due to UV exposure, therefore its efficacy decreases significantly. Phototoxic side-effects haven't been reported in clinical trials in relation to metronidazole. Unnecessary and prolonged use of this medication should be avoided.
Evidence suggests that metronidazole is carcinogenic in certain animal species. There is no evidence to date of a carcinogenic effect in human (see section 5.3).
This product contains methyl hydroxybenzoate (E218) and propyl hydroxybenzoate (E216) which may cause allergic reactions (possibly delayed). This product contains 30mg propylene glycol (E1520) in each gram which is equivalent to 3% w/w and may cause skin irritation.
Interaction with systemic medication is unlikely because absorption of metronidazole following cutaneous application of Rozex Gel is low. Nevertheless, it should be mentioned that disulfiram-like reactions have been reported in a small number of patients taking metronidazole and alcohol concomitantly. Oral metronidazole has been reported to potentiate the effect of warfarin and other coumarin anticoagulants, resulting in a prolongation of prothrombin time. The effect of topical metronidazole on prothrombin is not known. However, very rare cases of modification of the INR values have been reported with concomitant use of Rozex and coumarin anticoagulants.
Pregnancy
There is no experience to date with the use of Rozex Gel in pregnancy. In case of oral administration, metronidazole crosses the placental barrier and rapidly enters the foetal circulation. No foetotoxicity was observed after oral metronidazole in either rats or mice. However because animal reproduction studies are not always predictive of human response and since oral metronidazole has been shown to be a carcinogen in some rodents this drug should be used in pregnancy only if clearly needed.
Breast-feeding
After oral administration, Metronidazole is excreted in breast milk in concentrations similar to those found in the plasma, Metronidazole blood levels from topical administration are significantly lower than those achieved after oral administration. A decision should be made to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.
Rozex Gel has no influence on the ability to drive and use machines.
Because of the minimal absorption of metronidazole and consequently its insignificant plasma concentration after topical administration, the adverse experiences reported with the oral form of the drug have not been reported with Rozex Gel. Adverse reactions reported with Rozex Gel have been only local and mild.
System Organ Class
Frequency
Adverse drug reaction
Skin and subcutaneous tissue disorders
Common ( ≥ 1/100, < 1/10)
Dry skin, erythema, pruritus, skin discomfort (burning, pain of skin/stinging), skin irritation, worsening of rosacea.
Unknown frequency
Contact dermatitis, swelling face, skin exfoliation
Nervous system disorders
Uncommon (≥ 1/ 1,000, < 1/100)
Hypothesia, paraesthesia, dysgeusia (metallic taste)
Gastrointestinal disorders
Uncommon (≥ 1/ 1,000, < 1/100)
Nausea
Watery eyes have been reported if applied too closely to this area.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at https://yellowcard.mhra.gov.uk/ or search for MHRA Yellow Card in the Google Play or Apple App Store.
No data exists about overdosage in humans. Acute oral toxicity studies with a topical gel formulation containing 0.75% w/w metronidazole in rats have shown no toxic action with doses of up to 5 g of finished product per kilogram body weight, the highest dose used. This dose is equivalent to the oral intake of 12 tubes of 30g packaging Rozex Gel for an adult weighing 72 kg, and 2 tubes of Gel for a child weighing 12 kg.
Ask anything about Rozex 0.75% w/w Gel. The assistant answers only from this leaflet — if the leaflet does not cover it, it will say so. It does not give medical advice.
Answers come from the patient leaflet published on the electronic medicines compendium (emc). They are not medical advice. Ask a pharmacist or your GP if you are unsure. For urgent help call NHS 111, or 999 in an emergency.
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